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2-Methylhexane; 3-Methylhexane This page was last edited on 16 May 2022, at 14:52 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.
Theoretically 2-methylhexane also burns with a less sooty flame, emitting higher-frequency radiation; however, as heptane and 2-methylhexane differ by only one carbon atom, in terms of branching, both burn with a bright yellow flame when ignited. Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of ...
3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]
4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene .
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The following other wikis use this file: Usage on ar.wikipedia.org ميثيل هكسانامين; Usage on cs.wikipedia.org Dimethylamylamin; Usage on el.wikipedia.org
4-Methylethcathinone or 4-MEC is a chemical that bears a chemical resemblance to mephedrone. [3] Due to its similarity to mephedrone, it is thought to be a stimulant and entactogen drug of the phenethylamine , amphetamine , and cathinone chemical classes . [ 4 ]